CareLit · DOI-Nachweis · Aktuelle Neurologie
Identification of candidate genes in patients with amyotrophic lateral sclerosis by breakpoint characterisation
DOI 10.1055/s-2005-919642
Bibliografische Angaben
Nachweis in CareLit
Autor:innenJ.S Dullinger, J Prudlo, K Roemer, T Martin, E Göttert, K Zang, A.C Ludolph, C Menzel, V.M Kalscheuer, H.H Ropers, T Meyer
ZeitschriftAktuelle Neurologie
Ausgabe10/2005
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the selective loss of upper and lower motor neurons in the brain and spinal cord. Familial forms of ALS (FALS) account for 5–10% of all ALS patients and to date two disease genes, SOD1 and ALS2, have been identified. Genetic causes of the sporadic forms of ALS (SALS) are still unknown. We have investigated five patients with S…
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Zitierempfehlung
J.S Dullinger, J Prudlo, K Roemer, T Martin, E Göttert, K Zang, A.C Ludolph, C Menzel, V.M Kalscheuer, H.H Ropers, T Meyer (2005) Identification of candidate genes in patients with amyotrophic lateral sclerosis by breakpoint characterisation. Aktuelle Neurologie (10). https://doi.org/10.1055/s-2005-919642
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